A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3531520



Internal ID22400872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61389838..61390711hg38UCSC Ensembl
chr20:59964894..59965767hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38874
hg19874
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14298937, nssv14298938, nssv14298936
SamplesHG00512, NA19239, NA19240
Known GenesCDH4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3531520
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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